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血管生成素-2的泛癌和黑色素瘤特异性综合分析:预后价值、免疫微环境调节及ceRNA网络调控

Integrated pan-cancer and melanoma-specific analysis of angiopoietin-2: prognostic value, immune microenvironment modulation, and ceRNA network regulation.

作者信息

Ni Xuejun, Wan Xiaofen, Cai Beichen, Xie Hongteng, Chen Lu, Lin Qian, Ke Ruonan, Huang Tao, Ye Heyan, Shan Xiuying, Wang Biao

机构信息

Department of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.

Department of Plastic Surgery, National Regional Medical Center, Binhai Campus of The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350212, China.

出版信息

Discov Oncol. 2025 Sep 1;16(1):1666. doi: 10.1007/s12672-025-03448-5.

Abstract

OBJECTIVE

This research seeks to comprehensively explore the expression patterns of Angiopoietin-2 (ANGPT2) in pan-cancer and examine its relationship with clinical outcomes, tumor immune microenvironment dynamics, and biological functions, with particular emphasis on skin cutaneous melanoma (SKCM).

METHODS

Data from six databases, including UCSC Xena, TCGA, GTEx, TIMER2.0, GEPIA, and cBioPortal, were analyzed to assess ANGPT2 expression in pan-cancer. Immunohistochemical images were sourced from the HPA database. We explored the correlation between ANGPT2 expression and prognosis, diagnostic value, genetic alterations, and immune cell infiltration in cancers. Functional enrichment and gene set enrichment analyses were performed to uncover the biological roles of ANGPT2. Additionally, miRWalk, miRDB, Starbase 2.0 ENCORI, and Cytoscape were utilized to identify and construct the lncRNA-miRNA-ANGPT2 ceRNA regulatory network in SKCM.

RESULTS

Our comprehensive pan-cancer analysis revealed that ANGPT2 undergoes genetic alterations in several tumor types, including mutations, amplifications, and deep deletions. ANGPT2 expression varies across cancers, with high levels detected in 21 tumor types. ANGPT2 demonstrated significant diagnostic and prognostic value in various cancers. Genes related to ANGPT2 in cancers with high expression were found to be involved in critical pathways such as tumor angiogenesis, growth factor signaling, extracellular matrix (ECM) structure, and cell surface receptor activation. In addition, ANGPT2 was found to modulate the immune microenvironment in multiple tumors, promoting immune evasion and contributing to tumor progression, particularly in SKCM. A lncRNA-miRNA-ANGPT2 ceRNA regulatory network was identified, which may play a role in SKCM progression.

CONCLUSIONS

ANGPT2 demonstrates potential as a biomarker for cancer diagnosis and prognosis, with evidence suggesting its involvement in immune microenvironment regulation and associated gene networks. Therapeutic approaches targeting ANGPT2, either as a stand-alone treatment or in combination with immunotherapies, could offer new and effective strategies for future cancer treatments.

摘要

目的

本研究旨在全面探索血管生成素-2(ANGPT2)在泛癌中的表达模式,并研究其与临床结局、肿瘤免疫微环境动态变化及生物学功能的关系,尤其关注皮肤黑色素瘤(SKCM)。

方法

分析来自UCSC Xena、TCGA、GTEx、TIMER2.0、GEPIA和cBioPortal这六个数据库的数据,以评估ANGPT2在泛癌中的表达。免疫组化图像来自HPA数据库。我们探讨了ANGPT2表达与癌症预后、诊断价值、基因改变及免疫细胞浸润之间的相关性。进行功能富集和基因集富集分析以揭示ANGPT2的生物学作用。此外,利用miRWalk、miRDB、Starbase 2.0 ENCORI和Cytoscape识别并构建SKCM中的lncRNA-miRNA-ANGPT2 ceRNA调控网络。

结果

我们全面的泛癌分析表明,ANGPT2在几种肿瘤类型中发生基因改变,包括突变、扩增和深度缺失。ANGPT2在不同癌症中的表达各不相同,在21种肿瘤类型中检测到高水平表达。ANGPT2在各种癌症中显示出显著的诊断和预后价值。在高表达癌症中与ANGPT2相关的基因被发现参与关键途径,如肿瘤血管生成、生长因子信号传导、细胞外基质(ECM)结构和细胞表面受体激活。此外,发现ANGPT2在多种肿瘤中调节免疫微环境,促进免疫逃逸并导致肿瘤进展,尤其是在SKCM中。识别出一个lncRNA-miRNA-ANGPT2 ceRNA调控网络,其可能在SKCM进展中发挥作用。

结论

ANGPT2显示出作为癌症诊断和预后生物标志物的潜力,有证据表明其参与免疫微环境调节及相关基因网络。靶向ANGPT2的治疗方法,无论是作为单一治疗还是与免疫疗法联合使用,都可为未来癌症治疗提供新的有效策略。

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